Canonical Allele Identifier: CA2259200385
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665180_39665181delinsCG , CM000679.2:g.39665180_39665181delinsCG GRCh38
NC_000017.10:g.37821433_37821434delinsCG , CM000679.1:g.37821433_37821434delinsCG GRCh37
NC_000017.9:g.35074959_35074960delinsCG NCBI36
NG_008892.1:g.4835_4836delinsCG , LRG_210:g.4835_4836delinsCG
NG_042278.1:g.2200_2201delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-180_-179delinsCG ENSP00000312624.2:n.-180_-179delinsCG